Concurrent Developmental Regression and Neurocognitive Decline in a Child With De Novo CHD8 Gene Mutation-Reference-Cited by-同舟云学术

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Concurrent Developmental Regression and Neurocognitive Decline in a Child With De Novo CHD8 Gene Mutation

Published:2024-05 Issue: Volume:154 Page:1-3
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Paik Kyung Eun^ORCID,Mooneyham GenaLynne C.

Publisher

Elsevier BV

Reference15 articles.

1. Genetic mechanisms of regression in autism spectrum disorder;Tammimies;Neurosci Biobehav Rev,2019

2. Disruptive CHD8 mutations define a subtype of autism early in development;Bernier;Cell,2014

3. The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8;Dingemans;Transl Psychiatry,2022

4. A de novo variant of CHD8 in a patient with autism spectrum disorder;Alotaibi;Discoveries (Craiova),2020

5. De novo variants in the Helicase-C domain of CHD8 are associated with severe phenotypes including autism, language disability and overgrowth;An;Hum Genet,2020

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